Latest regulatory affairs Jobs

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for hematological malignancies, collaborating with a multidisciplinary team to ensure patient safety, scientific integrity, and regulatory compliance. This role involves medical monitoring, data review, and strategic partnerships with thought leaders in the oncology field.

GSK United States

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the end-to-end development of oncology drugs.

GSK

Hybrid Permanent

Precision Medicine Director

The Precision Medicine Director leads biomarker and diagnostic strategy development for global clinical programs in neuroscience, ensuring alignment with regulatory and clinical objectives. This role involves leading cross-functional teams, designing patient selection approaches, and supporting regulatory submissions. The position operates at the intersection of clinical development, diagnostics, and precision medicine, with a strong focus on scientific rigor and compliance.

Novartis London, United Kingdom

Hybrid Permanent

Precision Medicine Director

Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingNovartis is unable to offer relocation support: please only apply if accessible.The Precision Medicine Director is responsible for developing and executing precision medicine strategies aligned to disease area and clinical program objectives. This role leads...

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes specialized monitoring, regulatory support, and engaging with external stakeholders to drive strategic insights.

Pfizer United States

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of internal medicine assets, working with cross-functional teams to design and execute clinical trials. Key responsibilities include creating clinical development plans, ensuring regulatory compliance, and collaborating with external partners to advance Pfizer's clinical programs.

Pfizer

On-site Permanent

Director, Quality Assurance (Diagnostics & Devices)

Director, Quality Assurance (Diagnostics & Devices)Cambridge, UK (3 days on site per week)About AstraZenecaAstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases....

AstraZeneca Cambridge, United Kingdom

Senior Strategy Director (Senior Consultant) – Clinical Development – Evinova

This role involves leading the development and implementation of AI and digital health strategies to transform clinical development processes. The Senior Strategy Director will act as a trusted advisor, designing digital solutions for patient recruitment, remote monitoring, and data collection while driving innovation through AI. They will lead cross-functional teams, shape operating models, and ensure digital tools are integrated into clinical protocols with a focus on measurable value and patient outcomes.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

This role involves leading the development, qualification, and validation of cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, GLP/GCP-compliant data from clinical samples, contribute to regulatory documentation, and collaborate with cross-functional teams and external partners. Emphasis is placed on scientific rigor, innovation in assay design, and mentoring junior staff within a regulated, collaborative laboratory environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Automation Engineer, Laboratory Automation & Biobanking

This role involves designing and optimizing automated workflows for clinical biomarker assays using advanced liquid handling systems and Hamilton platforms. The engineer will integrate automation with data systems like LIMS, develop AI-enhanced laboratory workflows, and ensure compliance with GLP/GCLP standards. A key focus is building scalable, digitally connected laboratory ecosystems to support high-throughput sample management and biobanking operations.

Moderna Oxford, United Kingdom

Hybrid Permanent

Field Service Engineer (Omagh, Enniskillen, border regions)

This role involves providing frontline technical support for Roche's diagnostic products in the Omagh, Enniskillen, and border regions. Responsibilities include troubleshooting, preventative maintenance, technical training, and ensuring regulatory compliance. The position requires a strong technical background and the ability to work effectively in a fast-paced, customer-focused environment.

Roche

On-site Permanent